Safety and Efficacy of Oral NXC-736 in Adult Participants With Moderate and Severe Alopecia Areata

Recruiting Phase 2 Interventional Study
Alopecia Areata
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
19 – 65
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
73 (estimated)
Sponsor
NEXTGEN Bioscience · Industry
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About This Trial

The purpose of this study is to evaluate the safety and efficacy of NXC-736 monotherapy in participants with severe alopecia areata (AA).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Men or women between ≥19 and ≤65 years of age at the time of informed consent * Moderate and severe alopecia areata as assessed by a SALT score of 25% ≤ SALT \< 95% at Screening and Day 1/Baseline * Current episode of hair loss for ≥6 months but \<8 years * Stable disease cond…
Contacts

Heesun Kim

82-31-606-3220

flower@nextgenbio.co.kr

CONTACT

YangHye Park

yhpark@nextgenbio.co.kr

CONTACT